Polymers with low gel content and enhanced gas-fading

ABSTRACT

A polymer stabilizing composition comprising a sterically hindered phenol and a phosphite that provides low gel content and enhanced resistance to gas-fading. The stabilizer composition is particular useful for stabilizing polyethylene homopolymers and copolymers, such as linear low density polyethylenes produced from metallocene catalyst. The sterically hindered phenol is selected from the group consisting of 1,3,5-tris-(4-tert-butyl-3-hydroxy-2,6-dimethylbenzyl)isocyanurate, 1,3,5-tris-(3,5-dicyclohexyl-4-hydroxybenzyl)isocyanurate, 1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanurate, 1,3,5-tris(4-t-butyl-3-hydroxy-2,6-dimethylbenzyl)-1,3,5-Triazine-2,4,6-(1H,3H,5H)-trione, and 1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)-2,4,6-trimethylbenzene. The phosphite preferably is a liquid phosphite composition comprising two or more alkylated aryl phosphites.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of U.S. patent applicationSer. No. 11/787,531, filed Apr. 16, 2007, which claims priority to U.S.Provisional Application No. 60/815,819, filed Jun. 20, 2006. Each ofthese applications is incorporated herein by reference in its entirety.

This application is also a continuation-in-part of U.S. application Ser.No. 12/534,000, filed Jul. 31, 2009. This application is also acontinuation-in-part of U.S. application Ser. No. 12/534,010, filed Jul.31, 2009. This application is also a continuation-in-part of U.S.application Ser. No. 12/534,019, filed Jul. 31, 2009. This applicationis also a continuation-in-part of U.S. application Ser. No. 12/534,025,filed Jul. 31, 2009. This application is also a continuation-in-part ofU.S. application Ser. No. 12/534,035, filed Jul. 31, 2009. Thisapplication is also a continuation-in-part of U.S. application Ser. No.12/534,051, filed Jul. 31, 2009. This application is also acontinuation-in-part of U.S. application Ser. No. 12/534,043, filed Jul.31, 2009. This application also claims priority to U.S. ProvisionalApplication Nos. 61/230,658, 61/230,654 and 61/230,652, the entirecontents and disclosure of which are hereby incorporated by reference.

FIELD OF INVENTION

The present invention relates to novel compositions of stabilizers forpolymers that demonstrate low gel content and enhanced gas-fading. Morespecifically, the stabilizers comprise a sterically hindered phenol anda phosphite for stabilizing polyolefins.

BACKGROUND OF THE INVENTION

Polymers, e.g., polyolefins, polyvinyl halides, polyesters, polyamides,nitrile polymers, styrenic polymers and acrylate polymers, andelastomeric materials such as butadiene rubber, polyisoprene etc., areinherently unstable and susceptible to thermal oxidative degradation.Thus, these polymers and elastomeric material often requirestabilization during melt processing. Exemplary stabilizers includephenolic antioxidants, hindered amine light stabilizers, ultravioletlight absorbers, organophosphites, antioxidants, metal salts of fattyacids, hydrotalcites, metal oxides, epoxidized oils, hydroxylamines,amine oxides, lactones, and thiosynergists.

Organophosphites are used broadly in the stabilization of polyolefins asnon-discoloring antioxidants during melt processing, fabrication, andlong term applications. Stabilization strategy of various polyethyleneresins depends on the type (HDPE, LDPE, LLDPE, etc.), manufacturingprocess (gas-phase, slurry, solution), and catalyst (Ziegler-Natta,Chromium, metallocene, etc.) employed in the polymer production. Oftentimes, the molar ratio of phosphite to hindered phenolics and theneutralizer package is dependent on the polymer grade. It is a commoncommercial practice to use combinations of sterically hindered phenolsand phosphites in various molar ratios as a stabilizer system forpolyethylene. Commonly used sterically hindered phenols includetetrakismethylene (3,5-di-t-butyl-4-hydroxylhydrocinnamate) methane,octyl-3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate,bis(octadecyl)hydroxylamine,3,5-bis(1,1-dimethylethyl)-4-hydroxy-benzenepropanoic acid and2,6-di-t-butyl-4-ethyl-phenol. Commonly used phosphites includetris-nonylphenyl phosphite (TNPP) andtris(2,4-di-t-butylphenyl)phosphite, commercially sold under the tradenames Alkanox™ 240 (Chemtura Corporation, Middlebury, Conn., USA),Irgafos™ 168 (Ciba Specialty Chemicals Corporation, Tarrytown, N.Y.,USA), or Doverphos™ S-480 (Dover Chemical Corp, Dover, Ohio, USA).

TNPP and tris(2,4-di-t-butylphenyl)phosphite are commonly used inconjunction with octyl-3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate formelt stabilization of polyethylene. However, combinations of phosphiteswith octyl-3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate exhibit poor gasfading and high gel content when incorporated in polyethylene resins.Poor gas fading and high gel content render these stabilizers unsuitablefor film applications. Without being bound to theory, it is believedthat gels are small regions of high molecular weight polymers or looselycrosslinked polymers formed in the reactor and/or extruder, and aredifficult to remove once formed. The gels are a common problem for lowdensity polyethylenes and polyvinyl chlorides, and may cause distortionsin film applications. Some prior attempts have been made to reduce gelcontent by adding anti-gel agents, such as polyethylene glycols/oxidesor ethoxylated linear alcohols, as described in U.S. Pat. No. 4,540,538.

Thus, the need exists for safe and effective stabilizers that caneffectively stabilize polymer resins and compositions againstdegradation.

SUMMARY OF THE INVENTION

The present invention, in one embodiment, is directed to a stabilizingcomposition for polyolefins comprising: (1) a sterically hinderedphenol; and (2) a phosphite composition comprising at least twodifferent phosphites of the following: (i) a tris(dialkylaryl)phosphite,(ii) a tris(monoalkylaryl)phosphite, (iii) abis(dialkylaryl)monoalkylaryl phosphite, and (iv) abis(monoalkylaryl)dialkylaryl phosphite; wherein the phosphitecomposition is a liquid at ambient conditions.

The sterically hindered phenol may be selected from the group consistingof 1,3,5-tris-(4-tert-butyl-3-hydroxy-2,6-dimethylbenzyl)isocyanurate,1,3,5-tris-(3,5-dicyclohexyl-4-hydroxybenzyl)isocyanurate,1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanurate,1,3,5-tris(4-t-butyl-3-hydroxy-2,6-dimethylbenzyl)-1,3,5-Triazine-2,4,6-(1H,3H,5H)-trione,and1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)-2,4,6-trimethylbenzene.

The phosphite composition may comprise from 0.1 to 20 wt. % of thetris(dialkylaryl) phosphite, based on the total weight of the phosphitecomposition; from 20 to 70 wt. % of the tris(monoalkylaryl)phosphite;from 2 to 20 wt. % of the bis(dialkylaryl) monoalkylaryl phosphite, andfrom 15 to 60 wt. % of the bis(monoalkylaryl) dialkylaryl phosphite.

In another embodiment, there is provided an article comprising: a) apolyolefin selected from the group consisting of polyethylenehomopolymers, polyethylene copolymers, polypropylene homopolymers, andpolypropylene copolymers; and b) an effective amount of a stabilizingcomposition. The stabilizing composition comprises (1) a stericallyhindered phenol; and (2) a phosphite composition comprising at least twodifferent phosphites of the following: (i) a tris(dialkylaryl)phosphite,(ii) a tris(monoalkylaryl)phosphite, (iii) abis(dialkylaryl)monoalkylaryl phosphite, and (iv) abis(monoalkylaryl)dialkylaryl phosphite; wherein the phosphitecomposition is a liquid at ambient conditions. Preferably, thepolyolefin is linear low density polyethylene produced from ametallocene catalyst.

In such embodiments, the article may have a gel content, the size of thegel being 200 μm to 400 μm, of from 0.01 to 0.5 gel per square meter(gel/m²) of film. Preferably, the composition has no detectable gelsized formations that are greater than 400 μm. Preferably, thecomposition is substantially free of anti-gel agents. In addition, thearticle may have a yellowness index after exposure to NO for 7 days ofless than 0, for 18 days of less than 0.7, for 25 days of less than 1.1,for 33 days of less than 1.7 or for 41 days of less than 2.5.

In one embodiment, is the article comprises from 250 to 5000 wppm of thestabilizing composition, based on the total weight of the article. Theweight ratio of the sterically hindered phenol to the phosphitecomposition may be from 1:1 to 1:20 and in one embodiment from 1:10 to1:20.

In yet another embodiment, there is provided an article comprising: (a)a polyolefin selected from the group consisting of polyethylenehomopolymers, polyethylene copolymers, polypropylene homopolymers, andpolypropylene copolymers; and (b) an effective amount of a stabilizingcomposition. The stabilizing composition comprises (1) a stericallyhindered phenol; and (2) a phosphite selected from the group consistingof triphenyl phosphites, diphenylalkyl phosphites, phenyldialkylphosphites, tris(nonyl-phenyl)phosphites, trilauryl phosphites,trioctadecyl phosphites, distearyl pentaerythritol diphosphites,tris(2,4-di-tert-butylphenyl)phosphites, diisodecyl pentaerythritoldiphosphites, bis(2,4-di-tert-butylphenyl)pentaerythritol diphosphitestristearyl sorbitol triphosphites, bis(2,4-dicumylphenyl)pentaerythritol diphosphites,tetrakis(2,4-di-tert-butylphenyl)-4,4′-biphenylene diphosphonites ormixtures thereof. In this aspect, the article has a gel content, the gelbeing size 200 to 400 μm, of from 0.01 to 0.5 gel per square meter(gel/m²) of the article.

DETAILED DESCRIPTION OF THE INVENTION Introduction

The present invention relates to the stabilization of polymers using aneffective amount of a stabilizing composition comprising a stericallyhindered phenol and a phosphite, preferably a liquid phosphite. Thestabilizer composition is particular useful for stabilizing polyolefins,such as polyethylenes and polypropylenes. The effective amount of asterically hindered phenol and a phosphite of the invention contributesto increase color stability of the polyolefin when exposed to NO_(x).Surprisingly and unexpectedly, the effective amount of the stericallyhindered phenol and the phosphite further reduces gel content of thepolyolefins. These improved properties lead to improved performance inthe articles produced from the polyolefins.

A. Polymers

The polymers stabilized by the stabilizing compositions of the inventionmay be a polyethylene homopolymer or copolymer, or a polypropylenehomopolymer or copolymer. Although the present invention is discussed interms of polyethylene and polypropylene, other polymers known in theart, such as polyolefin homopolymers and copolymers, thermoplastics,rubbers, polyesters, polyurethanes, polyalkylene terephthalates,polysulfones, polyimides, polyphenylene ethers, styrenic polymers andcopolymers, polycarbonates, acrylic polymers, polyamides, polyacetals,halide-containing polymers, and biodegradable polymers are contemplatedby embodiments of the present invention.

In one embodiment, the polymers, typically ethylene based polymers, havea density in the range of from 0.86 g/cc to 0.97 g/cc, preferably in therange of from 0.88 g/cc to 0.965 g/cc, more preferably in the range offrom 0.900 g/cc to 0.96 g/cc, even more preferably in the range of from0.905 g/cc to 0.95 g/cc, yet even more preferably in the range from0.910 g/cc to 0.940 g/cc, and most preferably greater than 0.915 g/cc.The polymers of the invention may have a narrow, wide or bimodalmolecular weight distribution, a weight average molecular weight tonumber average molecular weight (Mw/Mn) of from about 1.5 to about 15,particularly from about 2 to about 10, more preferably from about 2.2 toabout 8, even more preferably from about 2.2 to about 5, and mostpreferably from about 2.5 to about 4. In one embodiment, the polymers ofthe present invention may have a tailored molecular weight distribution.The ratio of Mw/Mn can be measured by gel permeation chromatographytechniques well known in the art. The polymers of the present invention,in one embodiment, have a melt index (MI) or (12), as measured byASTM-D-1238-E, in the range from 0.01 to 1000 g per 10 mins, morepreferably from about 0.01 to about 100 g per 10 mins, even morepreferably from about 0.1 to about 50 g per 10 mins, and most preferablyfrom about 0.1 to about 10 g per 10 mins. The polymers of the invention,in one embodiment, have a melt index ratio (I21/I2) (I21 is measured byASTM-D-1238-F) of from 10 to 25, e.g., from 15 to 5. The polymers of theinvention, in a preferred embodiment, have a melt index ratio (121/12)(121 is measured by ASTM-D-1238-F) of from preferably greater than 25,more preferably greater than 30, even more preferably greater that 40,still even more preferably greater than 50 and most preferably greaterthan 65.

Non-limiting polymers include ethylene based polymers such as linear lowdensity polyethylene (LLDPE), low density polyethylene (LDPE),copolymers of ethylene and olefins having 3 or more carbon atoms, e.g.,3-12 carbon atoms, and propylene based polymers such as polypropylenepolymers including atactic, isotactic, and syndiotactic polypropylenepolymers, and propylene copolymers such as propylene random, block orimpact copolymers. In addition, polymers of polyethylene include highdensity polyethylene (HDPE), mixtures with other olefins such aspolypropylene with polyethylene (for example PP/HDPE, PP/LDPE) andmixtures of different types of polyethylene (for example LDPE/HDPE), mayalso be used. Also useful are copolymers of monoolefins and diolefinswith each other or with other vinyl monomers, such as, for example,ethylene/propylene, LLDPE and its mixtures with LDPE,propylene/butene-1, ethylene/hexene, ethylene/ethylpentene,ethylene/heptene, ethylene/octene, propylene/isobutylene,ethylene/butane-1, propylene/butadiene, ethylene/alkyl acrylates,ethylene/alkyl methacrylates, ethylene/vinyl acetate (EVA) orethylene/acrylic acid copolymers (EAA) and their salts (ionomers) andterpolymers of ethylene with propylene and a diene, such as hexadiene,dicyclopentadiene or ethylidene-norbornene; as well as mixtures of suchcopolymers and their mixtures with polymers mentioned above, for examplepolypropylene/ethylene propylene-copolymers, LDPE/EVA, LDPE/EAA,LLDPE/EVA, and LLDPE/EAA. As one skilled in the art would readilyappreciate, the polyethylene polymers used herein, e.g., LLDPE, cancontain various comonomers such as, for example, 1-butene, 1-hexene and1-octene comonomers.

The polymers used in combination with stabilizing compositions of thepresent invention are produced using a variety of polymerizationprocesses including solution, high-pressure, slurry and gas phase usingfree radical polymerization or various catalysts including, for example,Ziegler-Natta, single-site, metallocene, Phillips-type (chromium-based)catalysts, TNZ (DuPont) or Standard Oil Indiana. Polyethylene and/orpolypropylene polymers may be produced by, for example, polymerizationof olefins in the presence of Ziegler-Natta catalysts, optionally onsupports such as, for example, MgCl₂, chromium salts and complexesthereof, silica, silica-alumina and the like. The olefin polymers mayalso be produced utilizing chromium catalysts or single site catalysts,e.g., metallocene catalysts such as, for example, cyclopentadienecomplexes of metals such as Ti and Zr. Exemplary metallocene catalystare described in U.S. Pat. Nos. 4,827,064, 4,892,851, 4,912,272,5,012,020, 5,126,303, 5,296,434, 5,324,800, 5,731,254 6,706,828, and6,858,767, the entire contents and disclosure of which are incorporatedby reference.

In another embodiment, the polyethylene or polypropylene polymer maycomprise a biodegradable polymer or compostable polymer. Biodegradablepolymers are those in which the degradation results from the action ofnaturally occurring microorganisms, such as bacteria, fungi and algae.Compostable polymers undergoes degradation by biological processesduring composting to yield CO₂, water, inorganic compounds and a biomassat a rate consistent with other compostable materials. Typically thebiodegradable or compostable polymers are derived from plant sources andare synthetically produced. Examples of biodegradable or compostablepolymers include poly(glycolic acid) (PGA), poly(lactic acid) (PLA), andco-polymers thereof. Biodegradable or compostable polymers may also bederived from a blend of starch of a plant and a conventionalpetroleum-based polymer. For example, the biodegradable polymer may beblended with a polyolefin.

Although several polyethylenes and polypropylenes are described aswithin the scope of the present invention, in one embodiment, thepolymer is linear-low density polyethylene (LLDPE) that is anethylene-hexene or ethylene-octene copolymer having a density of 0.88 to0.94 g/cc, e.g., from 0.9 to 9.4 g/cc or from 0.91 to 9.4 g/cc and meltflow index of from 0.3 to 150 g per 10 min, e.g., from 0.6 to 15 g per10 min or from 0.8 to 3 g per 10 min. In one embodiment the LLDPE isproduced with a metallocene catalyst (mLLDPE). In one embodiment theLLDPE has a wide molecular weight distribution of from 2.8 to 8.

B. Stabilizing Compositions

The stabilizing compositions of the present invention generally comprisea sterically hindered phenol and a phosphite, preferably a liquidphosphite. As discussed above, a stabilizing amount or effective amountof the sterically hindered phenol and liquid phosphite compositions ofthe invention may be used as stabilizers for various types of polymerresins. As used herein, by “stabilizing amount” and an “effectiveamount” it is meant when the polymer resins containing the stabilizingcomposition of the invention shows improved stability in any of itsphysical or color properties in comparison to an analogous polymercomposition that does not include a stabilizing composition of theinvention. Examples of improved stability include improved stabilizationagainst, for example, molecular weight degradation, color degradation,and the like from, for example, melt processing, weathering, and/or longterm field exposure to air, heat, light, and/or other elements. In oneexample, improved stability is obtained in the form of one or both oflower initial color as measured by yellowing index (YI) and/or melt flowrate of the molten polymer or additional resistance to weathering, asmeasured, for example, by initial yellowing index, or by resistance toyellowing and change in color, when compared to a polymer without thestabilizer additives or a polymer with a conventional stabilizer. In oneexample, the improved stability is measured by low gel content, no blackspecs, and/or improved screen pack plugging.

In one embodiment, the stabilizing composition is added to the polymerin an amount from 250 to 5000 wppm, e.g., from 300 to 3000 wppm or from800 to 2600 wppm. The weight ratio of sterically hindered phenol tophosphite may be from 1:1 to 1:20, e.g., from 1:3 to 1:15 or from 1:5 to1:12. Although conventional stabilizing compositions use more phenol orequivalent amounts of phenol and phosphites, in one embodiment of thepresent invention, the amount of sterically hindered phenol may bereduced such that the weight ratio is from 1:10 to 1:20, e.g., from 1:12to 1:18 or from 1:12 to 1:15.

1. Sterically Hindered Phenolics

The sterically hindered phenols employed in the present inventiongenerally have two or more hydroxyl groups, e.g., three or more hydroxylgroups. In one embodiment, the sterically hindered phenol has thestructure as shown in compound I:

In another embodiment, the sterically hindered phenol has the structureas shown in compound II:

wherein: x is independently 0, 1, 2, or 3; R₁, R₂, and R₃ isindependently hydrogen, C₁-C₁₂ alkyl, and C₅-C₁₀ cycloalkyl, providedthat at least one of R₁, R₂, and R₃ is not hydrogen; and R₄ isindependently C₁-C₆ alkyl. Preferably x is either 0 or 1. In oneembodiment, at least one of R₁, R₂, and R₃ is a branched C₃-C₆ alkyl,e.g., branched butyl group or branched pentyl group. In one embodiment,at least one of R₁, R₂, and R₃ is methyl.

Suitable sterically hindered phenols of compound I include1,3,5-tris-(4-tert-butyl-3-hydroxy-2,6-dimethylbenzyl)isocyanurate,1,3,5-tris-(3,5-dicyclohexyl-4-hydroxybenzyl)isocyanurate,1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanurate commerciallyavailable as Anox™ IC-14 (Chemtura) also available as Irganox™ 3114(Ciba), and1,3,5-tris(4-t-butyl-3-hydroxy-2,6-dimethylbenzyl)-1,3,5-Triazine-2,4,6-(1H,3H,5H)-trionecommercially available as Lowinox™ 1790 (Chemtura) also available asCyanox™ 1790 (Cytec Industries).

Suitable sterically hindered phenols of compound II include1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)-2,4,6-trimethylbenzenecommercially available as Anox™ 330 (Chemtura) and also available asIrganox™ 1330 (Ciba) and Ethanox™ 330 (Albemale).

2. Phosphites

There are several different types of phosphites or phosphonites that maybe combined with the sterically hindered phenols discussed above, e.g.,compound I or II. In one embodiment the phosphite or phosphonite is aliquid. Phosphite performance may be affected by phosphorous content,hydrolytic stability, polymer compatibility, solubility, and loadinglevel.

a. Generally

In one embodiment, the phosphite or phosphonite, for example, may beselected from a triphenyl phosphite, diphenylalkyl phosphite,phenyldialkyl phosphite, tris(nonyl-phenyl)phosphite, trilaurylphosphite, trioctadecyl phosphite, distearyl pentaerythritoldiphosphite, tris(2,4-di-tert-butylphenyl)phosphite, diisodecylpentaerythritol diphosphite, bis(2,4-di-tert-butylphenyl)pentaerythritoldiphosphites tristearyl sorbitol triphosphite, bis(2,4-dicumylphenyl)pentaerythritol diphosphite,tetrakis(2,4-di-tert-butylphenyl)-4,4′-biphenylene diphosphonites ormixtures thereof. Specific suitable phosphite compounds includetriphenyl phosphite, tris(nonyl-phenyl)phosphite, trilauryl phosphite,trioctadecyl phosphite, distearyl pentaerythritol diphosphite,tris(2,4-di-tert-butylphenyl)phosphite, diisodecyl pentaerythritoldiphosphite, bis(2,4-di-tert-butylphenyl)pentaerythritol diphosphite,tristearyl sorbitol triphosphite, tris(dipropyleneglycol)phosphite,tetrakis(2,4-di-tert-butylphenyl)-4,4′-biphenylene diphosphonite, andmixtures thereof. Suitable commercially available phosphites include,for example, Naugalube™ TPP, Naugalube TPP, Alkanox™ 240, Ultranox™ 626,Naugard P, Weston™ 399, Weston TNPP, Weston 430, Weston 618F, Weston619F, Weston DPDP, Weston DPP, Weston PDDP, Weston PTP, Weston TDP,Weston TLP, Weston TPP, and Weston TLTTP (trilauryl trithio phosphite)made by Chemtura Corporation; Doverphos™ 4, Doverphos 4-HR, Doverphos4-HR Plus, Doverphos HiPure 4, and Doverphos S-9228 made by DoverChemical; and Hostanox PEPQ made by Clariant Chemicals.

b. Liquid Phosphite Compositions

In another preferred embodiment, the phosphite is a liquid phosphitecomposition comprising at least two different phosphites, e.g., at leastthree different phosphites, or at least four different phosphites,selected from the group consisting of a tris(dialkylaryl)phosphite, atris(monoalkylaryl)phosphite, a bis(dialkylaryl)monoalklyaryl phosphite,and a bis(monoalklyaryl)dialklyaryl phosphite, as described inco-pending U.S. application Ser. Nos. 11/787,531, 12/534,000,12/534,010, 12/534,019, 12/534,025, 12/534,035, 12/534,051, and12/534,043, and U.S. Provisional Application Nos. 61/230,658, 61/230,654and 61/230,652, the entire contents and disclosures of which are herebyincorporated by reference. Commercially available liquid phosphitecompositions include, for example, Weston™ 705 made by ChemturaCorporation.

In some preferred embodiments, the phosphite composition comprises atleast two different phosphites having the structure of formula III.

wherein R₅, R₆ and R₇ are independently selected alkylated aryl groupsand wherein the liquid phosphite composition is a liquid at ambientconditions. By “ambient conditions” it is meant room temperature, e.g.,25° C., and 1 atmosphere pressure.

The aryl moiety present in the phosphites of the liquid phosphitecomposition is preferably an aromatic moiety of from 6 to 18 carbonatoms, e.g., phenyl, naphthyl, phenanthryl, anthracyl, biphenyl,terphenyl, o-cresyl, m-cresyl, p-cresyl, and the like, preferablyphenyl. Each aromatic moiety is substituted with at least one C₁-C₁₈,e.g., C₄-C₁₀, or C₄-C₅ alkyl group. Preferably no aromatic moieties aresubstituted with any C₉ alkyl groups. The aromatic moieties may bemono-, di-, or tri-substituted in the ortho and/or para positions, butpreferably the phosphites themselves are not exclusivelymono-substituted, are not exclusively di-substituted, and are notexclusively tri-substituted.

In preferred embodiments, the invention is to a stabilized liquidphosphite composition comprising a liquid phosphite composition and anamine compound, wherein the liquid phosphite composition comprises atleast two of a tris(dialkylaryl)monophosphite, atris(monoalkylaryl)phosphite, a bis(dialkylaryl)monoalkylaryl phosphite,and a bis(monoalkylaryl)dialkylaryl phosphite, wherein the phosphitecomposition is a liquid at ambient conditions. Thus, the liquidphosphite composition comprises at least one phosphite that has at leastone aromatic moiety that is multiply substituted, such as abis(dialkylaryl)monoalkylaryl phosphite, a bis(monoalkylaryl)dialkylarylphosphite, or a tris(dialkylaryl)phosphite. The liquid phosphitecomposition also preferably includes at least one phosphite compound inwhich each aryl moiety is entirely monosubstituted, e.g., atris(monoalkylaryl)phosphite. The alkyl group in the alkylaryl phosphitecompounds preferably comprises a C₃-C₅ alkyl group, e.g., a C₄-C₅ alkylgroup, most preferably t-butyl and/or t-amyl, and the aryl grouppreferably comprises phenyl or cresyl, e.g., o-, m-, and/or p-cresyl.

More generally, the alkyl substituent(s) on the aryl moieties areselected from straight-chain or branched C₁-C₁₈ alkyl, e.g., C₁-C₈alkyl, C₄-C₆ alkyl, or C₄-C₅ alkyl, preferably C₄ alkyl or C₅ alkyl. Ina preferred embodiment, the alkyl substituent(s) is not C₈-C₁₀ alkyl,e.g., not C₉ alkyl. The alkyl substituent may include, for example,methyl, ethyl, propyl, butyl, amyl, hexyl, heptyl, octyl, nonyl(although less preferred), decyl, undecyl, dodecyl, tridecyl,tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, and isomersthereof. Most preferably, the alkyl group(s) are selected from butyl(especially sec-butyl and/or tert-butyl) and amyl groups (especiallysec-amyl, tert-amyl, and/or neo-amyl). As indicated above, in apreferred embodiment, the alkyl moieties do not include nonyl, meaningthe phosphite composition preferably comprises less than 50 wppm, e.g.,less than 10 wppm, or less than 5 wppm, nonyl substituted aryl phosphitecompounds, and most preferably no detectable nonyl substituted arylphosphite compounds. In addition, the phosphite composition preferablycomprises less than 50 wppm, e.g., less than 10 wppm, or less than 5wppm, nonylphenol. Most preferably, the phosphite composition comprisesno detectable nonylphenol.

In one embodiment, the phosphite composition is substantially free ofphosphite compounds having aryl groups that are substituted with alkylgroups having hydrogens in the α position. In preferred embodiments, atleast 95%, at least 98%, or at least 99% of the aryl moieties aresubstituted with alkyl groups having tertiary α-carbons, e.g.,tert-butyl and/or tert-amyl.

In one embodiment, R₅, R₆, and R₇ are independently selected alkylatedaryl groups of the structure of formula (IV):

wherein R₈, R₉, and R₁₀ are independently selected from the groupconsisting of hydrogen and straight or branched C₁-C₈ alkyl, e.g.,methyl, ethyl, propyl, butyl, amyl, hexyl, heptyl, octyl, and isomersthereof, e.g., isopropyl, tert-butyl, tert-amyl, neo-amyl, provided thatat least one of R₈, R₉, and R₁₀ is not hydrogen. In one embodiment R₈and R₁₀ are hydrogen, and R₉ is not hydrogen. In one embodiment, theortho alkyl groups, e.g., R₈ and R₁₀, have no α-hydrogen atoms. In oneembodiment, the ortho alkyl groups, e.g., R₈ and R₁₀, have tertiaryα-carbon atoms selected from the group consisting of tert-butyl andtert-amyl.

In one embodiment, R₈ and R₉ are independently selected from the groupconsisting of methyl, ethyl, propyl, butyl, amyl, hexyl, and isomersthereof, and R₁₀ is hydrogen. In another embodiment, R₈ and R₁₀ arehydrogen and R₉ is independently selected from the group consisting ofmethyl, ethyl, propyl, butyl, amyl, hexyl, and isomers thereof. In oneaspect of these embodiments, at least one of R₈, R₉, and R₁₀ are C₄ orC₅ alkyl, most preferably tert-butyl or tert-amyl.

In various optional embodiments, the alkylated aryl groups for R₅, R₆,and R₇ are provided as shown in Table 1. In some embodiments, the liquidphosphite composition, as described herein, may comprise any two or moreof these compounds in amounts sufficient for the phosphite compositionto be a liquid at ambient conditions.

TABLE 1 R₅ R₆ R₇ # R₈ R₉ R₁₀ R₈ R₉ R₁₀ R₈ R₉ R₁₀ 1 H t-butyl H H t-butylH H t-butyl H 2 t-butyl t-butyl H H t-butyl H H t-butyl H 3 t-butylt-butyl H t-butyl t-butyl H H t-butyl H 4 t-butyl t-butyl H t-butylt-butyl H t-butyl t-butyl H 5 H t-amyl H H t-amyl H H t-amyl H 6 t-amylt-amyl H H t-amyl H H t-amyl H 7 t-amyl t-amyl H t-amyl t-amyl H Ht-amyl H 8 t-amyl t-amyl H t-amyl t-amyl H t-amyl t-amyl H 9 H t-butyl HH t-butyl H H t-amyl H 10 H t-butyl H H t-amyl H H t-amyl H 11 t-butylt-butyl H H t-butyl H H t-amyl H 12 t-butyl t-butyl H H t-amyl H Ht-amyl H 13 t-butyl t-amyl H H t-amyl H H t-amyl H 14 t-amyl t-amyl H Ht-butyl H H t-amyl H 15 t-amyl t-amyl H H t-butyl H H t-butyl H 16t-butyl t-butyl H t-butyl t-butyl H H t-amyl H 17 t-butyl t-butyl Ht-butyl t-amyl H H t-butyl H 18 t-butyl t-amyl H t-butyl t-amyl H Ht-butyl H 19 t-amyl t-amyl H t-amyl t-amyl H H t-butyl H 20 t-butylt-amyl H t-butyl t-butyl H t-butyl t-butyl H 21 t-butyl t-amyl H t-butylt-amyl H t-amyl t-butyl H

In one embodiment, R₅, R₆, and R₇ are independently selected alkylatedaryl groups of the structure of formula (V):

wherein R₈, R₉, and R₁₀ are defined above and R₁₁ is hydrogen or methyl,provided that one of R₈, R₉, R₁₀, and R₁₁ is methyl and that at leasttwo of R₈, R₉, R₁₀, and R₁₁ are not hydrogen. Such phosphites may beformed, for example, by the reaction of one or more alkylated cresolcompounds, e.g., one or more of alkylated ortho-, meta-, and/orpara-cresol, with PCl₃.

In some preferred embodiments, the liquid phosphite compositioncomprises at least two phosphites selected from the group consisting oftris(4-t-butylphenyl)phosphite, tris(2-t-butylphenyl)phosphite,tris(2,4-di-t-butylphenyl)phosphite,bis(4-t-butylphenyl)-2,4-di-t-butylphenyl phosphite,bis(2,4-di-t-butylphenyl)-4-t-butylphenyl phosphite,bis(2-t-butylphenyl)-2,4-di-t-butylphenyl phosphite,bis(2,4-di-t-butylphenyl)-2-t-butylphenyl phosphite,tris(4-t-amylphenyl)phosphite, tris(2-t-amylphenyl)phosphite,tris(2,4-di-t-amylphenyl)phosphite,bis(4-t-amylphenyl)-2,4-di-t-amylphenyl phosphite,bis(2,4-di-t-amylphenyl)-4-tamylphenyl phosphite,bis(2-t-amylphenyl)-2,4-di-t-amylphenyl phosphite, andbis(2,4-di-t-amylphenyl)-2-tamylphenyl phosphite. In one embodiment, thephosphite composition does not comprise only phosphites that, whencombined in a composition, would result in a solid composition. Anexample of a phosphite that would result in a solid composition is oneproduced from the reaction of 2,4-di-t-butylphenol and2,4-di-t-amylphenol with phosphorus trichloride as described in U.S.Pat. No. 5,254,709.

In some embodiments, the phosphite composition has an overall phosphoruscontent that is equal to or greater than that of TNPP, e.g., at least4.5 wt. %, e.g., at least 4.8 wt. %, or at least 5.1 wt. %. In terms ofranges, the overall phosphorus content of the phosphite composition mayrange, from 4.5 to 10.0 wt. %, e.g., from 4.8 to 8.0 wt. %, or 5.1 to6.0 wt. %, based on the total weight of all phosphorous-containingcompounds in the phosphite composition.

As indicated above, the phosphite composition preferably comprises atleast two of the following: a tris(dialkylaryl)monophosphite, atris(monoalkylaryl)phosphite, a bis(dialkylaryl)monoalkylaryl phosphite,and a bis(monoalkylaryl)dialkylaryl phosphite, wherein the phosphitecomposition is a liquid at ambient conditions. The relative amounts ofthe respective phosphite components contained in the phosphitecomposition may vary somewhat so long as the phosphite compositionitself is a liquid at ambient conditions. Preferably, the phosphitecomposition comprises at least two of these compounds, at least three ofthese compounds, or all four of these compounds, in an amount greaterthan 80 wt. %, 90 wt. %, or 95 wt. %, based on the total weight of allphosphite compounds in the phosphite composition. Of course, a minoramount of other species, phosphite or non-phosphite, may be present,e.g., one or more of tris(2-tert-amylphenyl)phosphite,bis(2-tert-amylphenyl)-2,4-di-tert-amylphenyl phosphite,bis(2,4-di-tert-amylphenyl)-2-tert-amylphenyl phosphite, and the like.

The relative amounts of the respective phosphite components contained inthe liquid phosphite composition, as described herein, may vary somewhatso long as the phosphite composition is a liquid at ambient conditions.In terms of ranges, for example, the phosphite composition comprises atris(monoalkylaryl)phosphite, e.g., tris(4-t-amyl-phenyl)phosphite ortris(4-t-butyl-phenyl)phosphite, in an amount from 20 to 70 wt. %, e.g.,from 15 to 55 wt. %, or from 37 to 54 wt. %, and abis(monoalkylaryl)dialkylaryl phosphite, e.g.,bis(4-t-amyl-phenyl)-2,4-di-t-amyl-phenyl)phosphite orbis(4-t-butyl-phenyl)-2,4-di-t-butyl-phenyl)phosphite, in an amount from15 to 60 wt. %, e.g., from 31 to 50 wt. %, or from 34 to 45 wt. %.Optionally, the phosphite composition further comprises atris(dialkylaryl)phosphite, and/or bis(dialkylaryl)monoaryl phosphite.If present, the tris(dialkylaryl)phosphite, e.g.,tris(2,4-di-tert-amyl-phenyl)phosphite ortris(2,4-di-tert-butyl-phenyl)phosphite, preferably is present in anamount of from 0.1 to 20 wt. %, e.g., from 0.3 to 5 wt. %, or from 0.5to 1 wt. %. If present, the bis(dialkylaryl)monoaryl phosphite, e.g.,bis(2,4-di-tert-amyl-phenyl)-4-t-amyl-phenyl phosphite orbis(2,4-di-tert-butyl-phenyl)-4-t-butyl-phenyl phosphite, preferably ispresent in an amount of from 2 to 20 wt. %, e.g., from 4 to 20 wt. %, orfrom 5 to 10 wt. %. Unless otherwise indicated, weight percent (wt. %)is based on the total weight of the phosphite composition.

In terms of weight ratios, the phosphite composition optionally has aweight ratio of tris(monoalkylaryl)phosphites to the combination ofbis(monoalkylaryl)dialkylaryl phosphites, bis(dialkylaryl)monoalkylarylphosphites and tris(dialkylaryl)phosphites of from 1:4 to 7:3, e.g.,from 2:5 to 3:2, or from 3:5 to 6:5.

The phosphite composition optionally has a weight ratio ofbis(monoalkylaryl)dialkylaryl phosphites to the combination oftris(monoalkylaryl)phosphites, bis(dialkylaryl)monoalkylaryl phosphitesand tris(dialkylaryl)phosphites of from 1:6 to 3:2 e.g., from 1:3 to1:1, or from 1:2 to 2:3.

The phosphite composition optionally has a weight ratio ofbis(dialkylaryl)monoalkylaryl phosphites to the combination oftris(monoalkylaryl)phosphites, bis(monoalkylaryl)dialkylaryl phosphites,and tris(dialkylaryl)phosphites of from 1:50 to 2:5, e.g., from 1:30 to1:5, or from 1:20 to 1:9, or optionally less than 0.2:1, less than0.1:1, less than 0.05:1, or less than 0.02:1.

The phosphite composition optionally has a weight ratio oftris(dialkylaryl)phosphites to the combination ofbis(monoalkylaryl)dialkylaryl phosphites, bis(dialkylaryl)monoalkylarylphosphites and tris(monoalkylaryl)phosphites of from 1:10,000 to 2:5,e.g., from 1:5,000 to 1:20, or from 1:1,000 to 1:100, or optionally lessthan 0.02:1, less than 0.01:1, or less than 0.005:1.

Preferably, the liquid phosphite composition comprises at least two of atris(di-C₃-C₅ alkylaryl)phosphite, a tris(C₃-C₅ alkylaryl)phosphite, abis(di-C₃-C₅ alkylaryl) C₃-C₅ alkylaryl phosphite, and a bis(C₃-C₅alkylaryl) di-C₃-C₅ alkylaryl phosphite. Preferably the compositioncomprises each of the these phosphites in the following amounts: 1-5 wt% of the tris(di-C₃-C₅ alkylaryl)phosphite, 10-70 wt % of the tris(C₃-C₅alkylaryl)phosphite, 1-35 wt % of the bis(di-C₃-C₅ alkylaryl) C₃-C₅alkylaryl phosphite, and 5-70 wt % of the bis(C₃-C₅ alkylaryl) di-C₃-C₅alkylaryl phosphite.

As suggested above, the liquid phosphite compositions may becharacterized based on how the aryl moieties, e.g., phenyl moieties, aresubstituted, e.g., alkyl (e.g., t-butyl or t-amyl) substituted, as awhole. For example, in one embodiment, a majority of the aryl moietiesare mono substituted in the para-position, e.g., at least 50%, at least70%, or at least 90% mono substituted in the para-position, optionallyfrom 50 to 95%, e.g., from 55 to 90, or from 60 to 85% mono substitutedin the para-position, based on the number of aryl moieties in thephosphite composition. In other embodiments, some of the aryl moietiesare disubstituted, e.g., ortho- and para-disubstituted, at least inpart. Preferably at least 10% of the aryl moieties are ortho- andpara-disubstituted, e.g., at least 20% ortho- and para-disubstituted, orat least 50% ortho- and para-disubstituted, optionally from 5 to 50%ortho- and para-disubstituted, e.g., from 10 to 45% ortho- andpara-disubstituted, or from 15 to 40% ortho- and para-disubstituted,based on the total number of aryl moieties in the phosphite composition.In other embodiments, the ratio of monoalkylaryl groups to dialkylarylgroups ranges from 5:1 to 1:1, e.g., from 4:1 to 1:1, or from 3.5:1 to2:1.

Depending largely on how the phosphites are manufactured, the phosphitecompounds may be similarly substituted on each aryl moiety per molecule,e.g., some phosphite compounds may be exclusively monosubstituted, e.g.,para-substituted, and/or some phosphite compounds may be exclusivelydisubstituted, e.g., ortho and para disubstituted, provided that atleast some portion of the aryl moieties in the overall phosphitecomposition are mono-substituted and at least some portion of the arylmoieties in the overall phosphite composition are disubstituted. Forexample, some or all of the phosphite molecules may contain both monoand disubstituted aryl moieties. Additionally or alternatively, thephosphite composition may comprise phosphite molecules that areexclusively monosubstituted, e.g., para substituted and/or phosphitemolecules that are exclusively disubstituted, e.g., o/p disubstituted.

As indicated above, the liquid phosphite composition, as describedherein, includes phosphite compounds having aryl moieties that aremonoalkylated and dialkylated. Ideally, few if any of the aryl moietiesare trisubstituted. For example, fewer than 3 wt. % of the aryl moietiesare trisubstituted, e.g., fewer than 2 wt. %, or fewer than 1 wt. %.

Similarly, it is preferred that few, if any, of the aryl moieties aremonosubstituted in the ortho position. Preferably, the aryl moieties aremonosubstituted in the ortho position, if at all, in an amount less than3 wt. %, e.g., less than 2 wt. %, or less than 1 wt. %.

Preferably, the phosphite composition has a low level or issubstantially free of phenolics (e.g., phenols, cresols or xylenols),whether alkylated or unalkylated, which are referred to herein as “freephenolics” when contained in the phosphite composition. In terms ofamounts, the phosphite composition preferably comprises less than 5 wt.%, e.g., less than 3 wt. %, or less than 1 wt. %, of free phenolics,based on the total weight of the phosphite composition. Any freephenolics, for example, may be removed by distillation. Extremely lowlevels of free phenolics may be achieved, for example, by employing awiped-film molecular (Short-Path) still, wiped film evaporator (WFE),thin film evaporator, or similar equipment. In terms of amounts, thephosphite composition may comprise less than 0.5 wt. %, e.g., less than0.2 wt. %, or less than 0.1 wt. %, of free phenolics, based on the totalweight of the phosphite composition.

In other cases, a minor amount of free phenolics may be beneficial, forexample, as a viscosity reducing agent. Thus, the phosphite compositionmay comprise a minor amount of free phenolics, e.g., from 1 to 4 weightpercent, e.g., from 2 to 3 weight percent, based on the total weight ofthe phosphite composition.

In addition, the phosphite composition is preferably substantially freeof phosphite compounds having unsubstituted aryl moieties, e.g.,triphenylphosphites, bis(phenyl)alkylphenyl phosphites, orbis(alkylphenyl)phenyl phosphites. In terms of amounts, the phosphitecomposition preferably comprises less than 2 wt. %, e.g., less than 1wt. %, or less than 0.5 wt. %, phosphite compounds having at least oneunsubstituted aryl moiety, based on the total weight of the phosphitecomposition.

As indicated above, the phosphite composition is a liquid at ambientconditions. As used herein, by “liquid,” it is meant that the phosphitecomposition remains liquid after at least three “freeze/thaw” cycles asopposed to “meta-stable liquids,” which do not remain liquid after threeor fewer cycles. A freeze/thaw cycle is defined as follows: 1) Anambient temperature composition is stirred for 0.5 hours; 2) The stirredcomposition is then refrigerated at about 5° C. for three days; and 3)The refrigerated composition is then brought to ambient temperature andheld at ambient for 3 days. Upon completion of step 3, the compositionis checked for solids content, e.g., crystallization. Completion ofsteps 1-3 defines one freeze/thaw cycle.

As noted above, one feature of the phosphite composition is that it isin liquid physical form at room temperature. This is clearly surprising,given that the prior art teaches several examples of solid phosphitecompositions, the components of which are separately solids at ambientcondition, (See JP 59030842; WO 9303092; CA 2,464,551). In contrast, thephosphite composition discussed herein is liquid even though theindividual components are solid. Table 2 provides the melting points ofseveral different individual phosphite compounds that may be included inthe stabilized phosphite composition.

TABLE 2 Phosphite Melting Point tris(4-tert-butylphenyl)phosphite 75-76°C. tris(2,4-di-tert-butylphenyl)phosphite 181-184° C.bis(4-tert-butylphenyl)-2,4-di-tert-butylphenyl phosphite 63-65° C.bis(2,4-di-tert-butylphenyl)-4-tert-butylphenyl phosphite 100-103° C.tris(4-tert-amylphenyl)phosphite 52-54° C.tris(2,4-di-tert-amylphenyl)phosphite 103° C.

The viscosity of the phosphite composition may vary depending on therelative amounts of the various phosphite compounds contained therein.In some exemplary embodiments, the phosphite composition has a viscosityless than 11,000 cSt, e.g., less than 7,300 cSt, less than 5,000 cSt,less than 3,000 cSt, or less than 2850 cSt, these viscosities beingmeasured at 30° C. In terms of ranges, viscosity of the composition mayrange from 1 cSt to 15,000 cSt, from 100 cSt to 12,000 cSt, from 500 cStto 10,000 cSt, from 500 cSt to 6,500 cSt, from 500 cSt to 5,000 cSt,from 500 cSt to 3,000 cSt, from 1,000 cSt to 4,000 cSt, from 1,500 cStto 3,500 cSt, from 2,000 cSt to 3,000 cSt, or from 2,000 to 2,800 cSt,these viscosities being measured at 30° C.

In one embodiment, the liquid phosphites, including the phosphitecomposition includes one or more hydrolytic stabilizers. Suitablehydrolytic stabilizers include triethanolamine, triisopropanolamine,diethanolamine, diisopropanolamine, and tetraisopropanolethylenediamine.In another aspect the hydrolytic stabilizers includeoctyl-bis(2-ethanol)amine, nonyl-bis(2-ethanol)amine,decyl-bis(2-ethanol)amine, undecyl-bis(2-ethanol)amine,dodecyl-bis(2-ethanol)amine, tridecyl-bis(2-ethanol)amine,tetradecyl-bis(2-ethanol)amine, pentadecyl-bis(2-ethanol)amine,hexadecyl-bis(2-ethanol)amine, heptadecyl-bis(2-ethanol)amine,octadecyl-bis(2-ethanol)amine, octyl-bis(2-propanol)amine,nonyl-bis(2-propanol)amine, decyl-bis(2-propanol)amine,undecyl-bis(2-propanol)amine, dodecyl-bis(2-propanol)amine,tridecyl-bis(2-propanol)amine, tetradecyl-bis(2-propanol)amine,pentadecyl-bis(2-propanol)amine, hexadecyl-bis(2-propanol)amine,heptadecyl-bis(2-propanol)amine, octadecyl-bis(2-propanol)amine, andisomers thereof. Commercially available hydrolytic stabilizers includeArmostat™ 300 and Armostat 1800 manufactured by Akzo Nobel Polymers.Additional hydrolytic stabilizers include epoxies such as epoxidizedsoybean oil (ESBO) commercially available as Drapex™ 39, Drapex 392,Drapex 4.4, and Drapex 6.8 (Chemtura Corp.).

C. Other Liquid Phosphites

In yet another one embodiment, the phosphite is a liquidtris(mono-alkyl)phenyl phosphite ester or a liquid mixture of liquidtris(mono-alkyl)phenyl phosphite esters, as described in U.S. Pat. No.7,468,410, the entire contents and disclosures of which are herebyincorporated by reference. In particular, the phosphite may betris(3-t-butylphenyl)phosphite, tris(2-sec-butylphenyl)phosphite, ortris(4-sec-butylphenyl)phosphite. In one embodiment, the liquid mixturecomprises different phosphites, one of which istris(3-t-butylphenyl)phosphite, tris(2-sec-butylphenyl)phosphite, ortris(4-sec-butylphenyl)phosphite and the other of which istris(3-t-butylphenyl)phosphite, tris(2-sec-butylphenyl)phosphite,tris(4-sec-butylphenyl)phosphite, tris(2-t-butylphenyl)phosphite,tris(4-t-butylphenyl)phosphite, or tris(2,4-di-t-butylphenyl)phosphite.

3. Other Additives

In addition to the sterically hindered phenol and the phosphite, theremay be one or more additives and stabilizers that are preferably presentin an amount effective to improve composition stability. The one or moreadditives and stabilizers include additional phenolic antioxidants,aromatic amines, hydroxylamines, alkylamine-N-oxides, lactones, andthioethers, hindered amine light stabilizers (HALS), the ultravioletlight absorbers, alkaline metal salts of fatty acids, hydrotalcites,metal oxides, epoxidized soybean oils, the hydroxylamines, the tertiaryamine oxides, lactones, thermal reaction products of tertiary amineoxides, and the thiosynergists. In one embodiment, the total amount ofadditives, including the sterically hindered phenol and the liquidphosphite, may from 0.025 wt % to 20 wt %, e.g., from 0.1 to 5 wt %, orfrom 0.3 to 3 wt %, based on the total weight the polymer and additives.

In one embodiment, the amount of each component in the stabilizingcomposition, based on the total weight percent of the polymer, is shownin Table 3.

TABLE 3 Preferred Component Range Range Stabilizers of Present Invention0.025-0.5 wt %    0.08-0.26 wt % Additional Phenolic Antioxidants 0-3.0wt % 0.001-2.0 wt % UV or light stabilizers 0-3.0 wt % 0.001-2.0 wt %Metal deactivators 0-3.0 wt % 0.001-2.0 wt % Peroxide scavengers 0-3.0wt % 0.001-2.0 wt % Polyamide stabilizers 0-3.0 wt % 0.001-2.0 wt %Basic co-stabilizers 0-3.0 wt % 0.001-2.0 wt % Nucleating and clarifyingagents 0-3.0 wt % 0.001-2.0 wt % Aminoxy propanoate 0-3.0 wt % 0.001-2.0wt %

The stabilizer compositions of the invention or the resulting stabilizedpolymer compositions optionally also comprise additional phenolicantioxidants that are blended or mixed with the sterically hinderedphenols of the present invention. The additional phenolic antioxidantsinclude the following:

(i) Alkylated monophenols, for example:2,6-di-tert-butyl-4-methylphenol, 2-tert-butyl-4,6-dimethylphenol,2,6-di-tert-butyl-4-ethylphenol, 2,6-di-tert-butyl-4-n-butylphenol,2,6-di-tert-butyl-4-isobutylphenol, 2,6-dicyclopentyl-4-methylphenol,2,6-bis(α-methylbenzyl)-4-methylphenol,2-(α-methylcyclohexyl)-4,6-dimethylphenol,2,6-dioctadecyl-4-methylphenol, 2,4,6-tricyclohexyphenol, and2,6-di-tert-butyl-4-methoxymethylphenol. Commercially availablealkylated monophenols include Lowinox™ 624 and Naugard™ 431 made byChemtura Corp. Other phenols are commercially available as BHEB fromNanjing Datang Chemical Co., Ltd.

(ii) Alkylated hydroquinones, for example,2,6-di-tert-butyl-4-methoxyphenol, 2,5-di-tert-butyl-hydroquinone,2,5-di-tert-amyl-hydroquinone, and 2,6-diphenyl-4-octadecyloxyphenol.Commercially available alkylated hydroquinones include Lowinox AH25 madeby Chemtura.

(iii) Hydroxylated thiodiphenyl ethers, for example,2,2′-thio-bis-(6-tert-butyl-4-methylphenol),2,2′-thio-bis-(4-octylphenol),4,4′-thio-bis-(6-tert-butyl-3-methylphenol), and4,4′-thio-bis-(6-tert-butyl-2-methylphenol). Commercially availablehydroxylated thiodiphenyl ethers include Lowinox TMB6, and Lowinox TBP6made by Chemtura.

(iv) Alkylidene-bisphenols, for example,2,2′-methylene-bis-(6-tert-butyl-4-methylphenol),2,2′-methylene-bis-(6-tert-butyl-4-ethylphenol),2,2′-methylene-bis-(4-methyl-6-(α-methylcyclohexyl)phenol),2,2′-methylene-bis-(4-methyl-6-cyclohexylphenol),2,2′-methylene-bis-(6-nonyl-4-methylphenol),2,2′-methylene-bis-(6-nonyl-4-methylphenol),2,2′-methylene-bis-(6-(α-methylbenzyl)-4-nonylphenol),2,2′-methylene-bis-(6-(alpha,alpha-dimethylbenzyl)-4-nonyl-phenol),2,2′-methylene-bis-(4,6-di-tert-butylphenol),2,2′-ethylidene-bis-(6-tert-butyl-4-isobutylphenol),4,4′-methylene-bis-(2,6-di-tert-butylphenol),4,4′-methylene-bis-(6-tert-butyl-2-methylphenol),1,1-bis-(5-tert-butyl-4-hydroxy-2-methylphenol)butane,1,1-bis(2-methyl-4-hydroxy-5-tert-butylphenyl)butane,2,2′-isobutylidene-bis(4,6-dimethylphenol),2,6-di-(3-tert-butyl-5-methyl-2-hydroxybenzyl)-4-methylphenol,1,1,3-tris-(5-tert-butyl-4-hydroxy-2-methylphenyl)butane,1,1-bis-(5-tert-butyl-4-hydroxy-2-methylphenyl)-3-dodecyl-mercaptobutane,ethyleneglycol-bis-(3,3-bis-(3′-tert-butyl-4′-hydroxyphenyl)-butyrate)-di-(3-tert-butyl-4-hydroxy-5-methylphenyl)-dicyclopentadiene,anddi-(2-(3′-tert-butyl-2′hydroxy-5′methyl-benzyl)-6-tert-butyl-4-methylphenyl)terephthalate.Commercially available alkylidene-bisphenols include Lowinox 22M46,Lowinox WSP, Lowinox 44B25, Naugard 536, Naugawhite™, and Lowinox 221B46made by Chemtura.

(v) Acylaminophenols, for example, 4-hydroxylauric acid anilide,4-hydroxy-stearic acid amilide,2,4-bis-octylmercapto-6-(3,5-tert-butyl-4-hydroxyanilino)-s-triazine,and octyl-N-(3,5-di-tert-butyl-4-hydroxyphenyl)-carbamate.

(vi) Esters of beta-(3,5-di-tert-butyl-4-hydroxyphenol)-propionic acidwith monohydric or polyhydric alcohols, for example, methanol,diethyleneglycol, octadecanol, triethyleneglycol, 1,6-hexanediol,pentaerythritol, neopentylglycol, tris-hydroxyethylisocyanurate,thiodiethyleneglycol, di-hydroxyethyl oxalic acid diamide. Such phenolsalso includetetrakis[methylene{3,5-di-tert-butyl-4-hydroxycinnamate}]methane.Commercially available esters include Anox 20, Anox 1315, Lowinox GP45,Naugalube 38, Naugalube 531, Anox PP18, Naugard PS48 and Naugard XL-1made by Chemtura.

(vii) Thio esters ofbeta-(5-tert-butyl-4-hydroxy-3-methylphenyl)-propionic acid withmonohydric or polyhydric alcohols, for example, methanol,diethyleneglycol, octadecanol, triethyleneglycol, 1,6-hexanediol,pentaerythritol, neopentylglycol, tris-hydroxyethyl isocyanurate,thiodiethyleneglycol, dihydroxyethyl oxalic acid diamide. Commerciallyavailable thio esters include Naugalube™ 15 and Anox 70 made byChemtura.

(viii) Amides of beta-(3,5-di-tert-butyl-4-hydroxyphenol)-propionic acidfor example,N,N′-di-(3,5-di-tert-butyl-4-hydroxyphenylpropionyl)-hexammethylen-diamine,N,N′-di-(3,5-di-tert-butyl-4-hydroxyphenylpropionyl)trimethylenediamine,N,N′-di-(3,5-di-tert-butyl-4-hydroxyphenylpropionyl)-hydrazine,N,N′-Hexamethylene bis[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionamide,and 1,2-Bis(3,5-di-tert-butyl-4-hydroxyhydrocinnamoyl)hydrazine.Commercially available amides include Lowinox HD98 and Lowinox MD24 madeby Chemtura.

(ix) Other phenolic antioxidants include the following phenols.Polymeric phenols such as the reaction product of 4-methylphenol withdicyclopentadiene and isobutylene, commercially available as LowinoxCSTL; Chemtura. Alkylidene-poly-phenols, such as 1,3tris(3-methyl-4-hydroxyl-5-t-butyl-phenyl)-butane (Lowinox CA22;Chemtura). Thio phenols such as2,6-di-tert-butyl-4-(4,6-bis(octylthio)-1,3,5-triazin-2-ylamino)phenol(Irganox™ 565; Ciba), 4,6-bis(octylthiomethyl)-o-cresol (Irganox 1520;Ciba); 4,6-bis(dodecylthiomethyl)-o-cresol (Irganox 1726; Ciba).Hydroxylamines, such as bis(octadecyl)hydroxylamine (Irgastab™ FS 042;Ciba). Ester phenols include bis[3,3-bis(4-hydroxy-3-tert-butylphenyl)butanoic acid]glycol ester (Hostanox™ O3; Clariant Chemicals).Still other phenols include2-[1-(2-hydroxy-3,5-di-tert-pentylphenyl)ethyl]-4,6-di-tert-pentylphenylacrylate (Sumilizer GS; Sumitomo Chemical).

The stabilizer compositions and/or the resulting stabilized polymercompositions optionally also comprise one or more UV absorbers and/orlight stabilizers, such as the following:

(i) 2-(2′-hydroxyphenyl)-benzotriazoles, for example, the 5′-methyl-,3′5′-di-tert-butyl-, 3′5′-di-tert-amyl-, 5′-tert-butyl-, 5′-tert-amyl-,5′(1,1,3,3-tetramethylbutyl)-, 5-chloro-3′,5′-di-tert-butyl-,5-chloro-3′-tert-butyl-5′methyl-, 3′-sec-butyl-5′tert-butyl-,4′-octoxy,3′,5′-ditert-amyl-3′,5′-bis-(α,α-dimethylbenzyl)-derivatives.Commercially available 2-(2′-hydroxyphenyl)-benzotriazoles includeLowilite™ 26, Lowilite 27, Lowilite 28, Lowilite 29, Lowilite 35,Lowilite 55, and Lowilite 234 made by Chemtura.

(ii) 2-Hydroxy-benzophenones, for example, the 4-hydroxy, 4-methoxy-,4-octoxy, 4-decyloxy-, 4-dodecyloxy-, 4-benzyloxy-, 2,4-dihydroxy-,4,2′,4′-trihydroxy- and 2′-hydroxy-4,4′-dimethoxy-derivative. Exemplary2-hydroxy-benzophenones include 2-hydroxy-4-methoxybenzophenone,2-hydroxy-4-ethoxybenzophenone, 2,4-dihydroxybenzophenone, and2-hydroxy-4-propoxybenzophenone. Commercially available2-(2′-hydroxyphenyl)-benzotriazoles include Lowilite 20, Lowilite 22,Lowilite 20S, and Lowilite 24 made by Chemtura.

(iii) Esters of substituted and unsubstituted benzoic acids for example,phenyl salicylate, 4-tert-butylphenyl-salicylate, octylphenylsalicylate, dibenzoylresorcinol, bis-(4-tert-butylbenzoyl)-resorcinol,benzoylresorcinol,2,4-di-tert-butyl-phenyl-3,5-di-tert-butyl-4-hydroxybenzoate andhexadecyl-3,5-di-tert-butyl-4-hydroxybenzoate.

(iv) UV absorbers and light stabilizers may also comprise acrylates, forexample, alpha-cyano-beta, beta-diphenylacrylic acid-ethyl ester orisooctyl ester, alpha-carbomethoxy-cinnamic acid methyl ester,alpha-cyano-beta-methyl-p-methoxy-cinnamic acid methyl ester or butylester, alpha-carbomethoxy-p-methoxy-cinnamic acid methyl ester,N-(beta-carbomethoxy-beta-cyano-vinyl)-2-methyl-indoline.

(v) Nickel compounds are also suitable UV absorbers and lightstabilizers. Exemplary nickel compounds include nickel complexes of2,2′-thio-bis(4-(1,1,1,3-tetramethylbutyl)-phenol), such as the 1:1 or1:2 complex, optionally with additional ligands such as n-butylamine,triethanolamine or N-cyclohexyl-diethanolamine, nickeldibutyldithiocarbamate, nickel salts of4-hydroxy-3,5-di-tert-butylbenzylphosphonic acid monoalkyl esters, suchas of the methyl, ethyl, or butyl ester, nickel complexes of ketoximessuch as of 2-hydroxy-4-methyl-penyl undecyl ketoxime, nickel complexesof 1-phenyl-4-lauroyl-5-hydroxy-pyrazole, optionally with additionalligands. Commercially available nickel compounds include Lowilite Q84(2,2′-Thiobis(4-tert-octyl-phenolato))-N-butylamine-Nichel(ll) made byChemtura.

(vi) Sterically hindered amines may be used as UV absorbers and lightstabilizers. Sterically hindered amines, for examplebis(2,2,6,6-tetramethylpiperidyl)-sebacate,bis-(1,2,2,6,6-pentamethylpiperidyl)-sebacate,n-butyl-3,5-di-tert-butyl-4-hydroxybenzyl malonic acidbis(1,2,2,6,6-pentamethylpiperidyl)ester, condensation product of1-hydroxyethyl-2,2,6,6-tetramethyl-4-hydroxy-piperidine and succinicacid, condensation product ofN,N′-(2,2,6,6-tetramethylpiperidyl)-hexamethylendiamine and4-tert-octylamino-2,6-dichloro-1,3,5-s-triazine,tris-(2,2,6,6-tetramethylpiperidyl)-nitrilotriacetate,tetrakis-(2,2,6,6-tetramethyl-4-piperidyl)-1,2,3,4-butane-tetra-carbonicacid, 1,1′(1,2-ethanediyl)-bis-(3,3,5,5-tetramethylpiperazinone). Suchamines include hydroxylamines derived from hindered amines, such asdi(1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl)sebacate: 1-hydroxy2,2,6,6-tetramethyl-4-benzoxypiperidine;1-hydroxy-2,2,6,6-tetramethyl-4-(3,5-di-tert-butyl-4-hydroxyhydrocinnamoyloxy)-piperidine; andN-(1-hydroxy-2,2,6,6-tetramethyl-piperidin-4-yl)-epsiloncaprolactam.Commercially available hindered amines include Lowilite 19, Lowilite 62,Lowilite 77, Lowilite 92 and Lowilite 94 made by Chemtura.

(vii) Oxalic acid diamides, for examples, 4,4′-dioctyloxy-oxanilide,2,2′-di-octyloxy-5′,5′-di-tert-butyloxanilide,2,2′-di-dodecyloxy-5′,5′di-tert-butyl-oxanilide,2-ethoxy-2′-ethyl-oxanilide, N,N′-bis(3-dimethylaminopropyl)-oxalamide,2-ethoxy-5-tert-butyl-2′-ethyloxanilide and its mixture with2-ethoxy-2′ethyl-5,4-di-tert-butyloxanilide and mixtures of o- andp-methoxy- as well as of o- and p-ethoxy-disubstituted oxanilides.

The polymer resins and phosphite compositions of the invention may alsoinclude one or more additional additives, including, for example, one ormore of the following:

(i) Metal deactivators, for example, N,N′-diphenyloxalic acid diamide,N-salicylal-N′-salicyloylhydrazine, N,N′-bis-salicyloylhydrazine,N,N′-bis-(3,5-di-tert-butyl-4-hydrophenylpropionyl)-hydrazine,salicyloylamino-1,2,4-triazole, bis-benzyliden-oxalic acid dihydrazide.

(ii) Peroxide scavengers, for example, esters of betathiodipropionicacid, for example the lauryl, stearyl, myristyl or tridecyl esters,mercaptobenzimidazole or the zinc salt of 2-mercaptobenzimidazole,zinc-dibutyldithiocarbamate, dioctadecyldisulfide,pentaerythritoltetrakis-(beta-dodecylmercapto)-propionate.

(iii) Polyamide stabilizers, for example copper salts in combinationwith iodides and/or phosphorus compounds and salts of divalent manganesemay also be included in the polymer resin and/or phosphite composition.

(iv) Basic co-stabilizers, for example, melamine, polyvinylpyrrolidone,dicyandiamide, triallyl cyanurate, urea derivatives, hydrazinederivatives, amines, polyamides, polyurethanes, hydrotalcites, alkalimetal salts and alkaline earth metal salts of higher fatty acids, forexample, Ca stearate, calcium stearoyl lactate, calcium lactate, Znstearate, Zn octoate, Mg stearate, Na ricinoleate and K palmirate,antimony pyrocatecholate or zinc pyrocatecholate. Commercially availableco-stabilizers include Mark™ 6045, Mark 6045ACM, Mark 6055, Mark6055ACM, Mark 6087ACM, Mark 6102, Mark CE 345, Mark CE 350, and Mark CE387, made by Chemtura; and DHT-4ATM made by Kisuma Chemicals.

(v) Nucleating and clarifying agents, for example, metal salts of 4-tertbutylbenzoic acid, adipic acid, diphenylacetic acid, sorbitol andderivatives thereof, sodium benzoate, and benzoic acid.

(vi) Aminoxy propanoate derivatives such asmethyl-3-(N,N-dibenzylaminoxy)propanoate;ethyl-3-(N,N-dibenzylaminoxy)propanoate;1,6-hexamethylene-bis(3-N,N-dibenzylaminoxy)propanoate);methyl-(2-(methyl)-3(N,N-dibenzylaminoxy)propanoate);octadecyl-3-(N,N-dibenzylaminoxy)propanoic acid; tetrakis(N,N-dibenzylaminoxy)ethyl carbonyl oxymethy)methane;octadecyl-3-(N,N-diethylaminoxy)-propanoate;3-(N,N-dibenzylaminoxy)propanoic acid potassium salt; and1,6-hexamethylene bis(3-(N-allyl-N-dodecyl aminoxy)propanoate).

(vii) Other additives, for example, plasticizers, lubricants,emulsifiers, pigments, optical brighteners, flameproofing agents,anti-static agents, blowing agents and thiosynergists such asdilaurythiodipropionate or distearylthiodipropionate.

In one embodiment, the stabilizing composition of the present inventionis substantially free of anti-gel agents, such as polyethyleneglycols/oxides or ethoxylated linear alcohols, and contains less than 5wppm of anti-gel agents or less than 2 wppm of anti-gel agents or noanti-gel agents. As used herein, anti-gel agents are those compoundsadded to the stabilizer mixture to reduce gel formation and does notinclude the stabilizing compositions of sterically hindered phenols andphosphites of the present invention.

Optionally in the polymer or polymeric resins there may also be from5-50 wt %, e.g., 10-40 wt % or 15-30 wt % of fillers and reinforcingagents, for example, calcium carbonate, silicates, glass fibers,asbestos, talc, kaolin, mica, barium sulfate, metal oxides andhydroxides, carbon black and graphite.

C. Applications

Polymers that are stabilized with a stabilizing composition comprising asterically hindered phenol and a liquid phosphite are useful in formingoperations such as film, sheet, and fiber extrusion and co-extrusion aswell as blow molding, injection molding and rotary molding. Filmsinclude blown or cast films formed by coextrusion or by laminationuseful as shrink film, cling film, stretch film, sealing films, orientedfilms, snack packaging, heavy duty bags, grocery sacks, general purposebags, carrier bags, food packaging films, baked and frozen foodpackaging, agriculture films, medical packaging, industrial liners, ormembranes, in food-contact or non-food contact applications. Fibers,such as those prepared by melt spinning, solution spinning and meltblown fiber operations, are used in woven or non-woven form to makefilters, diaper fabrics, medical garments, geotextiles, etc. Extrudedarticles include, for example, medical tubing, wire and cable coatings,geomembranes, and pond liners. Molded articles include single andmulti-layered constructions in the form of bottles, tanks, large hollowarticles, rigid food containers and toys, etc. In addition to the above,the stabilizer compositions may be used in various rubber based productssuch as tires, barriers and the like.

D. Improved Performance Characteristics

When the stabilizer compositions of the invention are incorporated intopolymeric compositions, the characteristics and/or properties of thepolymeric composition, for example, color stability, e.g., as measuredby yellowing index, gel content, melt flow index, and oxygen inductiontime, may be significantly improved. In addition, unlike solid phosphitecompositions, liquid phosphite compositions beneficially may beincorporated into polymeric compositions without melting.

In terms of improving color, the stabilizers of the present inventionprovide improved resistance to discoloration from gas fading, as setforth by AATCC 23 at a temperature of 60° C. Oxides of nitrogen (NOx) inthe atmosphere, caused by pollutants, can react with the stabilizers,especially phenolic stabilizers, to trigger discoloration whichincreases as the exposure time increase. The yellowness index, measuredby ASTM D1925, of the polymer stabilized with the stabilizers of thepresent invention demonstrates a value at 7 days of exposure to NOx ofless than 0, e.g., less than −0.5 or less than −0.9; at 18 days of lessthan 0.7, e.g., less than 0.1 or less than −0.3; at 25 days of less than1.2, e.g., less than 1.1 or less than 1; at 33 days of less than 1.8,e.g., less than 1.7 or less than 1.65; and at 41 days of less than 3,e.g., less than 2.5 or less than 2.4. This is a significant improvementover resins stabilized with conventional stabilizers.

Gel content may be measured by counting the number of 200 to 400 μm gelsized formations in a square meter of polymeric film. The polymersstabilized with stabilizers of the present invention preferably have agel content of 200 to 400 μm gel sized formations ranging from 0.01 to0.5 gel per square meter (gel/m²) of film, e.g., from 0.05 to 0.45gel/m², or from 0.1 to 0.42 gel/m². These gel contents obtained with thestabilizing compositions of the invention are significantly lower thanthose achieved using conventional stabilizers which typically have gelcontents of greater than 1 gel/m², e.g., greater than 2 gel/m², orgreater than 3 gel/m². In one embodiment, the polymers stabilized withthe stabilizing compositions of the invention have no detectable gelsize formations greater than 400 μm. Conventional stabilizers whichtypically have detectable amount of gel contents greater than 400 μm ofless than 5 gel/m², e.g., less than 2 gel/m² or less than 0.5 gel/m².

Without further elaboration, it is believed that one skilled in the artcan, using the description herein, utilize the present invention to itsfullest extent. The following examples are included to provideadditional guidance to those skilled in the art in practicing theclaimed invention. The examples provided are merely representative ofthe work that contributes to the teaching of the present application.Accordingly, these examples are not intended to limit the invention, asdefined in the appended claims, in any manner.

EXAMPLES

The present invention will be further understood in view of thefollowing non-limiting examples.

Example 1

LLDPE, which is an ethylene-hexene copolymer having a density of 0.918g/cc and melt flow index of 0.6 to 1.0 g per 10 mins, was stabilizedwith a 2150 wppm of1,3,5-tris(4-t-butyl-3-hydroxy-2,6-dimethylbenzyl)-1,3,5-Triazine-2,4,6-(1H,3H,5H)-trione(Lowinox 1790) and tris(nonyl-phenyl)phosphite (Weston TNPP). The LLDPEwas produced in a gas phase polymerization process using metallocenecatalyst.

Comparative Example A

LLDPE from Example 1 was stabilized with 2500 wppm ofoctadecyl-3-(3′,5′-di-tert-butyl-4′-hydroxyphenyl)propionate (Anox PP18)and tris(nonyl-phenyl)phosphite (Weston TNPP).

Comparative Example B

LLDPE from Example 1 was stabilized with 2000 wppm ofoctadecyl-3-(3′,5′-di-tert-butyl-4′-hydroxyphenyl)propionate (Anox PP18)and tris(2,4-di-tert-butylphenyl)phosphite (Alkanox 240).

Example 2

Surprisingly and unexpectedly, the gel content measurements of Example 1and Comparative Examples A and B demonstrated that Example 1 has asignificantly lower gel content compared with Comparative Examples A andB as summarized in Table 4 below. Example 1 and Comparative Examples Aand B did not contain any anti-gel agents.

TABLE 4 Gel Counts of 200 to Gel Counts of 400 μm Example 400 μm(gel/m²) or greater (gel/m²) 1 Less than 0.42 0 A 2.8-2.9 Less than 0.5B 3.6-3.7 Less than 0.5

Example 3

A gas fading analysis of Example 1 and Comparative Examples A and Bdemonstrated that Example 1 had low gas fading (AATCC 23) to NOx overthe test period as summarized in Table 5 below. The yellow index (YI) isdetermined by ASTM D1925.

TABLE 5 NOx Exposure Yellow Index (YI) (Days) Example 1 Comparative AComparative B 0 −1.099 −1.094 −0.896 7 −0.307 −0.662 0.259 18 0.6490.732 2.494 25 1.098 1.686 3.692 33 1.614 2.566 4.6 41 2.496 4.184 6.071

1. A stabilizing composition for polyolefins, comprising: (1) asterically hindered phenol; and (2) a phosphite composition comprisingat least two different phosphites selected from: (i) atris(dialkylaryl)phosphite, (ii) a tris(monoalkylaryl)phosphite, (iii) abis(dialkylaryl)monoalkylaryl phosphite, and (iv) abis(monoalkylaryl)dialkylaryl phosphite; wherein the phosphitecomposition is a liquid at ambient conditions.
 2. The composition ofclaim 1, wherein the sterically hindered phenol is selected from thegroup consisting of1,3,5-tris-(4-tert-butyl-3-hydroxy-2,6-dimethylbenzyl)isocyanurate,1,3,5-tris-(3,5-dicyclohexyl-4-hydroxybenzyl)isocyanurate,1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanurate,1,3,5-tris(4-t-butyl-3-hydroxy-2,6-dimethylbenzyl)-1,3,5-Triazine-2,4,6-(1H,3H,5H)-trione,and1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)-2,4,6-trimethylbenzene.3. The composition of claim 1, wherein the sterically hindered phenolhas the structure of compound I:

wherein: x is independently 0, 1, 2, or 3; R₁, R₂, and R₃ isindependently hydrogen, C₁-C₁₂ alkyl, and C₅-C₁₀ cycloalkyl, providedthat at least one of R₁, R₂, and R₃ is not hydrogen.
 4. The compositionof claim 1, wherein the sterically hindered phenol has the structure ofcompound II:

wherein: x is independently 0, 1, 2, or 3; R₁, R₂, and R₃ isindependently hydrogen, and C₁-C₁₂ alkyl, and C₅-C₁₀ cycloalkyl,provided that at least one of R₁, R₂, and R₃ is not hydrogen; and R₄ isindependently C₁-C₆ alkyl.
 5. The composition of claim 1, wherein thephosphite composition comprises: from 0.1 to 20 wt. % of thetris(dialkylaryl)phosphite; from 20 to 70 wt. % of thetris(monoalkylaryl)phosphite; from 2 to 20 wt. % of thebis(dialkylaryl)monoalkylaryl phosphite, and from 15 to 60 wt. % of thebis(monoalkylaryl)dialkylaryl phosphite, based on the total weight ofthe phosphite composition.
 6. The composition of claim 1, wherein thetris(dialkylaryl)phosphite is tris(2,4-di-tert-amyl-phenyl)phosphite ortris(2,4-di-tert-butyl-phenyl)phosphite.
 7. The composition of claim 1,wherein the tris(monoalkylaryl)phosphite istris(4-t-amyl-phenyl)phosphite or tris(4-t-butyl-phenyl)phosphite. 8.The composition of claim 1, wherein the bis(dialkylaryl)monoalkylarylphosphite is bis(2,4-di-tert-amyl-phenyl)-4-t-amyl-phenyl phosphite orbis(2,4-di-tert-butyl-phenyl)-4-t-butyl-phenyl phosphite.
 9. Thecomposition of claim 1, wherein the bis(monoalkylaryl)dialkylarylphosphite is bis(4-t-amyl-phenyl)-2,4-di-t-amyl-phenyl)phosphite orbis(4-t-butyl-phenyl)-2,4-di-t-butyl-phenyl)phosphite.
 10. Thecomposition of claim 1, wherein the composition is substantially free ofanti-gel agents.
 11. The composition of claim 1, wherein the weightratio of the sterically hindered phenol to the phosphite composition isfrom 1:1 to 1:20.
 12. The composition of claim 1, wherein the polyolefinis produced by free-radical polymerization, Ziegler-Natta catalysts,Phillips-type catalysts, single-site catalysts, and metallocenecatalysts.
 13. The composition of claim 1, wherein the polyolefin islinear low density polyethylene produced from a metallocene catalyst.14. An article, comprising: a) a polyolefin selected from the groupconsisting of polyethylene homopolymers, polyethylene copolymers,polypropylene homopolymers, and polypropylene copolymers; and b) aneffective amount of a stabilizing composition, comprising: (1) asterically hindered phenol; and (2) a phosphite composition comprisingat least two different phosphites selected from: (i) atris(dialkylaryl)phosphite, (ii) a tris(monoalkylaryl)phosphite, (iii) abis(dialkylaryl)monoalkylaryl phosphite, and (iv) abis(monoalkylaryl)dialkylaryl phosphite; wherein the phosphitecomposition is a liquid at ambient conditions.
 15. The article of claim14, wherein the article has a gel content of 200 to 400 μm gel sizedformations of from 0.01 to 0.5 gel per square meter (gel/m²) of film.16. The article of claim 14, wherein the article has no detectable gelsized formations that are greater than 400 μm.
 17. The article of claim14, wherein the article has a yellowness index after exposure to NOx for7 days of less than 0, for 18 days of less than 0.7, for 25 days of lessthan 1.1, for 33 days of less than 1.7 or for 41 days of less than 2.5.18. The article of claim 14, wherein the article comprises thestabilizing composition in an amount from 250 to 5000 wppm.
 19. Thearticle of claim 14, wherein the phosphite composition comprises: from0.1 to 20 wt. % of the tris(dialkylaryl)phosphite; from 20 to 70 wt. %of the tris(monoalkylaryl)phosphite; from 2 to 20 wt. % of thebis(dialkylaryl)monoalkylaryl phosphite, and from 15 to 60 wt. % of thebis(monoalkylaryl)dialkylaryl phosphite, based on the total weight ofthe phosphite composition.
 20. An article, comprising: a) a polyolefinselected from the group consisting of polyethylene homopolymers,polyethylene copolymers, polypropylene homopolymers, and polypropylenecopolymers; and b) an effective amount of a stabilizing composition,comprising: (1) a sterically hindered phenol; and (2) a phosphiteselected from the group consisting of triphenyl phosphites,diphenylalkyl phosphites, phenyldialkyl phosphites,tris(nonyl-phenyl)phosphites, trilauryl phosphites, trioctadecylphosphites, distearyl pentaerythritol diphosphites,tris(2,4-di-tert-butylphenyl)phosphites, diisodecyl pentaerythritoldiphosphites, bis(2,4-di-tert-butylphenyl)pentaerythritol diphosphitestristearyl sorbitol triphosphites, bis(2,4-dicumylphenyl)pentaerythritoldiphosphites, tetrakis(2,4-di-tert-butylphenyl)-4,4′-biphenylenediphosphonites and mixtures thereof; wherein the article has a gelcontent of 200 to 400 μm gel sized formations of from 0.01 to 0.5 gelper square meter (gel/m²) of the article.
 21. The article of claim 20,wherein the article has no detectable gel sized formations that aregreater than 400 μm.
 22. The article of claim 20, wherein the articlehas a yellowness index after exposure to NOx for 7 days of less than 0,for 18 days of less than 0.7, for 25 days of less than 1.1, for 33 daysof less than 1.7 or for 41 days of less than 2.5.
 23. The article ofclaim 20, wherein the article comprises the stabilizing composition inan amount from 250 to 5000 wppm.